适体
化学
检出限
色谱法
互补DNA
镰刀菌
DNA
呕吐毒素
真菌毒素
食品科学
分子生物学
生物化学
植物
基因
生物
玉米赤霉烯酮
作者
Mei Wu,Zhi Yang,Longsheng Wang,Zhi-Chun Zhan,Chuan‐Chao Dai,Yan‐Zhen Mei
标识
DOI:10.1080/00032719.2023.2297298
摘要
Deoxynivalenol (DON) is the key virulence factor in Fusarium head blight. However, rapid and low-cost methods for DON are limited. Herein, a novel label-free GelRed-aptamer sensor was developed for the detection of DON. GelRed was embedded in double strain DNA (dsDNA) consisting of a single chain aptamer and its complementary DNA (cDNA), resulting in the increase of fluorescence intensity. However, DON preferentially combined with the aptamer and did not combine with its cDNA, which would result in the decrease in the formation of the GelRed/aptamer/cDNA complex, greatly reducing the fluorescence intensity. The samples were extracted from wheat, centrifuged, and filtered through a 0.22 μm membrane. Good linearity was obtained for DON from 3.13 to 313 mg L−1. The limit of quantitation (LOQ) for wheat samples was 6.07 mg L−1, providing a low cost method for DON compared with enzyme-linked immunosorbent assays. Experiments with spiked samples showed good recoveries from 92% to 105% with relative standard deviations less than 5.33% with analysis within 20 min. This method is simple and low cost with potential applications in agriculture and food.
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